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NCT02530333 · ClinicalTrials.gov registry record · NA

Differential Biomechanical Effects of an ACL Injury Prevention Program in Women's Basketball and Soccer Players

A NA study, sponsored by High Point University.

Completed
Registry status
NA
Development phase
99
Enrollment target

NCT02530333: Completed NA study, sponsored by High Point University.

NCT02530333 is a NA study that has completed, run by High Point University. The registered enrollment target is 99 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02530333, a NA study, has completed, sponsored by High Point University.

COMPLETED
Registry status
NA
Development phase
99 participants
Enrollment target

Study Summary

Anterior cruciate ligament injury programs are less successful in women's basketball than soccer players, yet the reason for this discrepancy is unknown. Thus, this study will recruit high school aged girl's basketball and soccer players, randomized teams into control and experimental groups, administer an ACL injury prevention program in the experimental group and compare the two groups on their lower extremity biomechanics before and after completion of the program. Biomechanical analyses will help determine the extent to which women's basketball and soccer players respond differently to a uniform injury prevention program, and whether this prevention program provides an adequate stimulus to improve lower extremity biomechanics during basketball-specific tasks.

Interventions

  • OTHER Neuromuscular Prevention Program

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2015-05
Est. Completion 2015-11
Phase NA
High Point University

10 total trials

What the finished NCT02530333 record still lists

NCT02530333 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 99 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Neuromuscular Prevention Program is the first listed.

NCT02530333 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02530333 about?

NCT02530333 is a clinical study titled "Differential Biomechanical Effects of an ACL Injury Prevention Program in Women's Basketball and Soccer Players". Anterior cruciate ligament injury programs are less successful in women's basketball than soccer players, yet the reason for this discrepancy is unknown. Thus, this study will recruit high school aged girl's basketball and soccer players, randomized teams into control and experimental groups, admini...

What is the current status of trial NCT02530333?

This trial is currently completed. It is a NA study. The enrollment target is 99 participants. The study started on 2015-05. Estimated completion is 2015-11.

What interventions are being tested in trial NCT02530333?

The interventions under investigation include: Neuromuscular Prevention Program (OTHER).

Who is sponsoring clinical trial NCT02530333?

This trial is sponsored by High Point University, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02530333's enrollment target sits among peer trials

99 920th of 2000 higher than 1,079 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02530333, the US trial registry maintained by the National Library of Medicine. NCT02530333 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.